Electrochemical properties of ultrasonically prepared Ni(OH)2 nanosheets in lithium cells

被引:21
作者
Caballero, A. [1 ]
Hernan, L. [1 ]
Morales, J. [1 ]
Cabanas-Polo, S. [2 ]
Ferrari, B. [2 ]
Sanchez-Herencia, A. J. [2 ]
Canales-Vazquez, J. [3 ]
机构
[1] Univ Cordoba, Dpto Quim Inorgan, Inst Univ Invest Quim Fina & Nanoquim, E-14071 Cordoba, Spain
[2] Inst Ceram & Vidrio ICV CSIC, Madrid 28049, Spain
[3] Univ Castilla La Mancha, Inst Energias Renovables, Albacete 02071, Spain
关键词
Nickel hydroxide; Nanosheets; Lithium batteries; Solid-electrolyte interface; NIO-NI NANOCOMPOSITE; ION BATTERIES; POROUS NIO; PERFORMANCE; ANODE; FABRICATION; ELECTRODES; REACTIVITY; GRAPHITE; LI;
D O I
10.1016/j.jpowsour.2013.04.033
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
The electrochemical behavior of beta-Ni(OH)(2) nanosheets in half-lithium cells was studied. The first discharge curve exhibited two well-defined plateaux giving two well-defined peaks in the CV curve. The plateaux were assigned to reduction of Ni in the nanosheets to metallic Ni and the formation of a solid electrolyte interface (SEI), respectively. By contrast, NiO exhibited a single peak. On further cycling, the curve shapes for beta-Ni(OH)(2) resembled those for NiO, but the peak assigned to Ni oxidation was shifted to higher voltages. Cycling the electrode made from the nanosheets over the potential range 3.0-0.0 V provided capacities above 1430 mAh g(-1) after the second cycle that were largely retained on further cycling. This surprisingly high capacity level substantially exceeds the theoretical capacity of Ni(OH)(2) and is twice the theoretical value for NiO. Removing the plateau assigned to SEI formation by limiting the lower potential to 0.85 V caused not only the expected decrease in discharge capacity, but also substantial capacity fading with cycling, which provides direct evidence for the central role of SEI formation. The unusually high capacity obtained is probably due to formation of the reversible interface as demonstrated by transmission electron microscopy (TEM) images of the discharged and charged electrode. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:366 / 371
页数:6
相关论文
共 25 条
[1]
Chemical composition and morphology of the elevated temperature SEI on graphite [J].
Andersson, AM ;
Edström, K .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2001, 148 (10) :A1100-A1109
[2]
Building better batteries [J].
Armand, M. ;
Tarascon, J. -M. .
NATURE, 2008, 451 (7179) :652-657
[3]
Capacity fade mechanisms and side reactions in lithium-ion batteries [J].
Arora, P ;
White, RE ;
Doyle, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (10) :3647-3667
[4]
A comparative study of synthetic graphite and Li electrodes in electrolyte solutions based on ethylene carbonate dimethyl carbonate mixtures [J].
Aurbach, D ;
Markovsky, B ;
Shechter, A ;
EinEli, Y ;
Cohen, H .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (12) :3809-3820
[5]
Effect of reaction conditions on size and morphology of ultrasonically prepared Ni(OH)2 powders [J].
Cabanas-Polo, S. ;
Suslick, K. S. ;
Sanchez-Herencia, A. J. .
ULTRASONICS SONOCHEMISTRY, 2011, 18 (04) :901-906
[6]
Facile ammonia-induced fabrication of nanoporous NiO films with enhanced lithium-storage properties [J].
Chen, Xin ;
Zhang, Naiqing ;
Sun, Kening .
ELECTROCHEMISTRY COMMUNICATIONS, 2012, 20 :137-140
[7]
Débart A, 2001, J ELECTROCHEM SOC, V148, pA1266, DOI 10.1149/1.1409971
[8]
Preparation and characterization of CoO used as anodic material of lithium battery [J].
Do, JS ;
Weng, CH .
JOURNAL OF POWER SOURCES, 2005, 146 (1-2) :482-486
[9]
An update on the reactivity of nanoparticles Co-based compounds towards Li [J].
Grugeon, S ;
Laruelle, S ;
Dupont, L ;
Tarascon, JM .
SOLID STATE SCIENCES, 2003, 5 (06) :895-904
[10]
Particle size effects on the electrochemical performance of copper oxides toward lithium [J].
Grugeon, S ;
Laruelle, S ;
Herrera-Urbina, R ;
Dupont, L ;
Poizot, P ;
Tarascon, JM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2001, 148 (04) :A285-A292